Associated Papers
SBIDDS Syndrome: A New Spoke of the Epigenetic Machinery Wheel.
Aleo S et al.
Molecular Syndromology, 2023
Novel PRMT7 mutation in a rare case of dysmorphism and intellectual disability.
Poquérusse J et al.
Journal of Human Genetics, 2022
Further delineation of the phenotype caused by loss of function mutations in PRMT7.
Valenzuela I et al.
European Journal of Medical Genetics, 2019
Prenatal and postnatal presentation of PRMT7 related syndrome: Expanding the phenotypic manifestations.
Birnbaum R et al.
American Journal of Medical Genetics. Part A, 2019
Expanding the clinical and molecular spectrum of PRMT7 mutations: 3 additional patients and review.
Agolini E et al.
Clinical Genetics, 2018
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